1-(4-Aminophenyl)-1,3,3-trimethyl-5-indanamine(CAS号:54628-89-6)

5(6)-氨基-1-(4-氨基苯基)-1,3,3-三甲基茚满

基本信息

1-(4-Aminophenyl)-1,3,3-trimethyl-5-indanamine

CAS号

54628-89-6

分子式

C18H22N2

分子量

266.39 g/mol

Quick Actions

基本物理性质

沸点

432.3°C at 760 mmHg

密度

1.091±0.06 g/cm3 (20 ºC 760 Torr),

闪点

257.9°C

折射率

1.615

SMILES

CC1(CC(C2=C1C=C(C=C2)N)(C)C3=CC=C(C=C3)N)C

InChI

InChI=1S/C18H22N2/c1-17(2)11-18(3,12-4-6-13(19)7-5-12)15-9-8-14(20)10-16(15)17/h4-10H,11,19-20H2,1-3H3

InChIKey

CGSKOGYKWHUSLC-UHFFFAOYSA-N

LogP

3.838300000000002

拓扑极性表面积

52.04 Ų

氢键供体/受体

4 / 2

复杂度

356

分类与用途

安全信息

查看安全信息

同义词与参考文献

英文

  • 1-(4-Aminophenyl)-2,3-dihydro-1,3,3-trimethyl-1H-inden-5-amine
  • 1H-Inden-5-amine,1-(4-aminophenyl)-2,3-dihydro-1,3,3-trimethyl-
  • MFCD18971260
  • 1-(4-aminophenyl)-1,3,3-trimethyl-2H-inden-5-amine
  • FT-0774684
  • SCHEMBL137367
  • 1-(4-Aminophenyl)-1,3,3-trimethyl-5-indanamine
  • BCP29464
  • NS00056278
  • 1H-Inden-5-amine, 1-(4-aminophenyl)-2,3-dihydro-1,3,3-trimethyl-
  • EINECS 259-261-6
  • 1-(4-Aminophenyl)-1,3,3-trimethyl-2,3-dihydro-1H-inden-5-amine
  • 54628-89-6
  • DTXSID30969898
  • PIDA
  • 1-(4-aminophenyl)-1,3,3-trimethyl-2,3-dihydro-1H-inden-5-amine

中文

  • 5(6)-氨基-1-(4-氨基苯基)-1,3,3-三甲基茚满
  • 1-(4-氨基苯基)-2,3-二氢-1,3,3-三甲基 -1H-茚-5-胺
  • 5(6)-1-(4-氨基苯基)-1,3,3-三甲基茚满
  • 1-(4-氨基苯基)-2,3-二氢-1,3,3-三甲基-1H-茚-5-胺

MDL_Number

MFCD18971260

CAS号

54628-89-6

供应商信息

供应商名称 会员等级 认证状态 主要类别 最小订购量 操作
中国中国 - 湖北清北云研医药科技有限责任公司
中国中国 - 湖北拓邦化工有限公司
中国中国 - 南通众合化工新材料有限公司
中国中国 - 上海瀚思化工有限公司
中国中国 - 陕西信瑞生物科技有限公司
中国中国 - 南京易普易达科技发展有限公司
德国德国 - Elektrowärme Gabbey
中国中国 - 上海卡恩医药科技有限公司

相关文献

A robust multifunctional ligand-controlled palladium-catalyzed carbonylation reaction in water

Kan Zhang, Ming-Ming Yang, Shan Xu, Hua-Ming Sun, Jin-Lei Zhang, Zi-Wei Gao, Wei-Qiang Zhang

2018-04-24 Communication

DOI: 10.1039/C8CC00324F

From zinco(ii) arsaketenes to silylene-stabilised zinco arsinidene complexes

Ernesto Ballestero-Martínez, Terrance J. Hadlington, Tibor Szilvási, Shenglai Yao, Matthias Driess

2018-04-16 Communication

DOI: 10.1039/C8CC01928B

Co-production of pure hydrogen, carbon dioxide and nitrogen in a 10 kW fixed-bed chemical looping system

Sebastian Bock, Robert Zacharias, Viktor Hacker

2020-01-02 Paper

DOI: 10.1039/C9SE00980A

Tessellation strategy for the interfacial synthesis of an anthracene-based 2D polymer via [4+4]-photocycloaddition

Renzeng Chen, Danbo Wang, Wenbo Hao, Feng Shao, Yingjie Zhao

2021-05-07 Communication

DOI: 10.1039/D1CC02179F

Chemoproteomics-based target profiling of sinomenine reveals multiple protein regulators of inflammation

Lianguo Chen, Hong-jian Wang, Teng-fei Ji, Chong-Jing Zhang

2021-05-06 Communication

DOI: 10.1039/D1CC01522B

In situ growth of all-inorganic perovskite nanocrystals on black phosphorus nanosheets

Hao Huang, Jia Li, Ya Yi, Jiahong Wang, Yihong Kang, Paul K. Chu, H. C. Ong, Xue-Feng Yu

2018-02-08 Communication

DOI: 10.1039/C8CC00029H

Metal–organic frameworks: preparation and applications in highly efficient heterogeneous photocatalysis

Van-Huy Nguyen, Shi-Rong Zhou, Shu-Yu Hsu, Jia-Xuan Tan

2019-11-22 Review Article

DOI: 10.1039/C9SE00972H

Contents list

Front/Back Matter

DOI: 10.1039/D0CC90139C

Biomaterials Science Emerging Investigators 2021

Maria E. Southall

2021-06-02 Editorial

DOI: 10.1039/D1BM90053F

Small size yet big action: a simple sulfate anion templated a discrete 78-nuclearity silver sulfur nanocluster with a multishell structure

Li-Ping Cheng, Zhi Wang, Qiao-Yu Wu, Hai-Feng Su, Tao Peng, Geng-Geng Luo, Yan-An Li, Di Sun, Lan-Sun Zheng

2018-02-07 Communication

DOI: 10.1039/C8CC00014J